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9-cis-12-trans-15-trans-Octadecatriensaeure | 21661-12-1

中文名称
——
中文别名
——
英文名称
9-cis-12-trans-15-trans-Octadecatriensaeure
英文别名
octadeca-9c,12t,15t-trienoic acid;9Z,12E,15E-octadecatrienoic acid;(9Z,12E,15E)-octadeca-9,12,15-trienoic acid
9-cis-12-trans-15-trans-Octadecatriensaeure化学式
CAS
21661-12-1
化学式
C18H30O2
mdl
——
分子量
278.435
InChiKey
DTOSIQBPPRVQHS-KYNNUBNZSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    5.9
  • 重原子数:
    20
  • 可旋转键数:
    13
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.61
  • 拓扑面积:
    37.3
  • 氢给体数:
    1
  • 氢受体数:
    2

文献信息

  • [EN] LYMPHATIC SYSTEM-DIRECTING LIPID PRODRUGS<br/>[FR] PROMÉDICAMENTS LIPIDIQUES ORIENTANT VERS LE SYSTÈME LYMPHATIQUE
    申请人:ARIYA THERAPEUTICS INC
    公开号:WO2019046491A1
    公开(公告)日:2019-03-07
    The present invention provides lymphatic system-directing lipid prodrugs, pharmaceutical compositions thereof, methods of producing such prodrugs and compositions, as well as methods of improving the bioavailability or other properties of a therapeutic agent that comprises part of the lipid prodrug. The present invention also provides methods of treating a disease, disorder, or condition such as those disclosed herein, comprising administering to a patient in need thereof a provided lipid prodrug or a pharmaceutical composition thereof.
    本发明提供了淋巴系统定向脂质前药,其制药组合物,制备这种前药和组合物的方法,以及改善作为脂质前药一部分的治疗剂的生物利用度或其他性质的方法。本发明还提供了治疗疾病、紊乱或症状的方法,包括向需要的患者施用所提供的脂质前药或其制药组合物。
  • [EN] LPXH TARGETING COMPOUNDS, COMPOSITIONS THEREOF, AND METHODS OF MAKING AND USING THE SAME<br/>[FR] COMPOSÉS DE CIBLAGE LPXH, LEURS COMPOSITIONS ET PROCÉDÉS DE FABRICATION ET D'UTILISATION ASSOCIÉS
    申请人:UNIV DUKE
    公开号:WO2021072369A1
    公开(公告)日:2021-04-15
    LpxH targeting compounds, compositions thereof, as well as methods for for making and using the same are disclosed herein. The LpxH target compounds typically have a structure pursuant to Formula (I) and/or a salt thereof, wherein Rb is selected from a single bond, C4 to C10 unsubstituted aryl, C4 to C10 substituted aryl, unsubstituted or substituted four to ten member heterocycle ring, C1 to C10 unsubstituted alkyl, and C1 to C10 substituted alkyl; Rc comprises hydrogen, halogen, -OH, -CO2CH3, -COOH, -CN2CF3, -CF3,-C2OH, -CONHOH, -CCOH, C4 to C10 unsubstituted aryl, C4 to C10 substituted aryl, unsubstituted or substituted four to ten member heterocycle ring, C1 to C10 unsubstituted alkyl, or C1 to C10 substituted alkyl; and Rd and Re are independently hydrogen, -OH, -COH, -COH, -COC, -COOH, Rf, or are taken together as an unsubstituted or substituted four to eight member nitrogen containing heterocycle ring.
    LpxH靶向化合物,其组合物,以及制备和使用这些化合物的方法在此披露。LpxH靶向化合物通常具有符合式(I)的结构和/或其盐,其中Rb从单键,C4到C10未取代芳基,C4到C10取代芳基,未取代或取代的四到十元杂环环,C1到C10未取代烷基,和C1到C10取代烷基中选择;Rc包括氢,卤素,-OH,-CO2CH3,-COOH,-CN2 ,-CF3,-C2OH,-CONHOH,-CCOH,C4到C10未取代芳基,C4到C10取代芳基,未取代或取代的四到十元杂环环,C1到C10未取代烷基,或C1到C10取代烷基;而Rd和Re独立地是氢,-OH,-COH,-COH,-COC,-COOH,Rf,或作为未取代或取代的四到八元含氮杂环环一起取代。
  • [EN] COMPOUNDS THAT INDUCE DEGRADATION OF ANTI-APOPTOTIC BCL-2 FAMILY PROTEINS AND THE USES THEREOF<br/>[FR] COMPOSÉS INDUISANT LA DÉGRADATION DE PROTÉINES ANTI-APOPTOTIQUES DE LA FAMILLE BCL-2 ET UTILISATION DE CES DERNIERS
    申请人:BIOVENTURES LLC
    公开号:WO2017184995A1
    公开(公告)日:2017-10-26
    The present disclosure provides compositions and methods for selectively killing senescent cells, wherein the composition comprises a compound of Formula (I) or a compound of Formula (II). The selective killing of senescent cells may delay aging and/or treat age-related disorders.
    本公开提供了一种用于选择性杀灭衰老细胞的组合物和方法,其中该组合物包括式(I)的化合物或式(II)的化合物。对衰老细胞的选择性杀灭可能延缓衰老和/或治疗与年龄相关的疾病。
  • [EN] MELAMPOMAGNOLIDE B DIMERS<br/>[FR] DIMÈRES DE MÉLAMPOMAGNOLIDE B
    申请人:UNIV ARKANSAS
    公开号:WO2016090166A1
    公开(公告)日:2016-06-09
    The present disclosure provides dimers of melampomagnolide B (MMB), including carbamate, carbonate, succinic amide, ester and carboxamide dimers of MMB. These derivatives are useful for treating cancer in humans, in particular in treating leukemia, including acute myelogenous leukemia (AML). A compound comprising Formula (1 ) wherein: Z is independently selected from the group consisting of CH2, O, C(O), and CH, wherein when Z is CH, Z is connected to Y via a double bond and Y is N.
    本公开提供了美拉波木内酯B(MMB)的二聚体,包括MMB氨基甲酸酯、碳酸酯、琥珀酰胺、酯和羧酰胺二聚体。这些衍生物对于治疗人类癌症特别有用,尤其是治疗白血病,包括急性髓性白血病(AML)。一种包含如下式(1)的化合物:其中:Z独立地选自由CH2、O、C(O)和CH组成的群,当Z为CH时,Z通过双键连接到Y,而Y为N。
  • MELAMPOMAGNOLIDE B DERIVATIVES
    申请人:Janganati Venumadhav
    公开号:US20150133444A1
    公开(公告)日:2015-05-14
    The present disclosure provides derivatives of melampomagnolide B (MMB), including carbonates, carbamates, and thiocarbamates. The derivatives may be synthesized via an MMB triazole intermediate. These derivatives are useful for treating cancer in humans.
    本公开提供了槲皮素B(MMB)的衍生物,包括碳酸酯、氨基甲酸酯和氨基甲酸酯。这些衍生物可以通过MMB三唑中间体合成。这些衍生物对于治疗人类癌症是有用的。
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